Cook G00220Recalls & reported problems
Cook Incorporated · Plastic 3-Way Stopcock · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002002203), received between Feb 27, 2017 and Feb 2, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Fracture1
- Leak/Splash1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 2, 2018Fracture; Fracture
IT WAS REPORTED THAT UPON INSPECTION IN THE HOSPITAL STORAGE AREA (PRIOR TO USE/ OPENING PACKAGING,) TWO THREE-WAY PLASTIC STOPCOCKS WERE OBSERVED TO BE CRACKED. ONE OF THE PACKAGES WAS OPENED TO FURTHER OBSERVE CRACKING OF THE DEVICE. THE DEVICES DID NOT COME INTO CONTACT WITH THE PATIENT. ANOTHER THREE-WAY PLASTIC STOPCOCK WAS UTILIZED TO SUCCESSFULLY COMPLETE THE PROCEDURE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7237290 ↗MalfunctionFeb 27, 2017Leak/Splash; Leak/Splash
IT WAS REPORTED, AFTER THE THREE-WAY PLASTIC STOPCOCK IS HOOKED UP, THE DEVICE LEAKS AND WAS NOTED TO BE CRACKED. THE STOPCOCK WAS REPLACED AND THE PROCEDURE WAS COMPLETED. NO ADDITIONAL INFORMATION HAS BEEN RECEIVED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6361465 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.